Saiardi A, Falasca P, Civitareale D
Istituto di Ricerche Farmacologiche Mario Negri, Consorzio Mario Negri Sud, S.Maria Imbaro, Italy.
Biochem Biophys Res Commun. 1994 Nov 30;205(1):230-7. doi: 10.1006/bbrc.1994.2654.
Thyrotropin, by binding its specific receptor on the plasma membrane of the thyrocyte, regulates thyroid function and differentiation. In FRTL5 cells, thyrotropin down-regulates the thyrotropin receptor (TSHr) promoter activity and induces the transcription of the alpha form of thyroid hormone receptor (TR-alpha 1). In this study we show that the thyrotropin receptor down-regulation, induced by thyrotropin, is mediated by TR-alpha 1. The thyroid hormone receptor binds, in vitro, the thyrotropin receptor minimal promoter and inhibits promoter activity in cotransfections experiments in CV 1 cells. The inhibition is achieved only in the presence of the thyroid hormone. The TSHr promoter mutated in the thyroid hormone receptor binding site does not bind TR, in vitro, and its activity is not inhibited, in cotransfection experiments, in CV 1 cells. The same mutation abolishes the TSH mediated down-regulation of the TSHr promoter activity in FRTL5 thyroid cells. These results support the hypothesis of a regulatory short loop of thyroid hormone in thyroid cells.
促甲状腺激素通过与甲状腺细胞浆膜上的特异性受体结合来调节甲状腺功能和分化。在FRTL5细胞中,促甲状腺激素下调促甲状腺激素受体(TSHr)启动子活性,并诱导甲状腺激素受体α型(TR-α1)的转录。在本研究中,我们表明促甲状腺激素诱导的促甲状腺激素受体下调是由TR-α1介导的。甲状腺激素受体在体外与促甲状腺激素受体最小启动子结合,并在CV-1细胞的共转染实验中抑制启动子活性。仅在甲状腺激素存在的情况下才能实现这种抑制。在甲状腺激素受体结合位点发生突变的TSHr启动子在体外不与TR结合,并且在CV-1细胞的共转染实验中其活性不受抑制。相同的突变消除了TSH介导的FRTL5甲状腺细胞中TSHr启动子活性的下调。这些结果支持甲状腺细胞中甲状腺激素调节短环的假说。